Phenotype #0000223098

Individual ID 00295528
Associated disease ?
Diagnosis/Initial osteogenesis imperfecta
Diagnosis/Definite osteogenesis imperfecta
Phenotype details -
Inheritance Familial, autosomal recessive
Age/Examination 32y (32 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset sp7
Protein -
Tumor/MSI -
Diagnosis/Criteria -
Owner name Muhammad Umair
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Muhammad Umair
Date created 2020-03-17 13:10:23 +01:00 (CET)
Date last edited 2020-03-19 13:58:02 +01:00 (CET)

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